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Article

Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.

PloS one - 1 Jan 2016

Gasca-Salas Carmen, Masellis Mario, Khoo Edwin, Shah Binit B, Fisman David, Lang Anthony E, Kleiner-Fisman Galit

Abstract excerpt

BACKGROUND: Mutations in granulin (PGRN) and tau (MAPT), and hexanucleotide repeat expansions near the C9orf72 genes are the most prevalent genetic causes of frontotemporal lobar degeneration. Although behavior, language and movement presentations are common, the relationship between genetic subgroup and movement disorder phenomenology is unclear. OBJECTIVE: We conducted a systematic review and meta-analysis of...

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Source

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Identifiers

PMID: 27100392
DOI: 10.1371/journal.pone.0153852
PMCID: PMC4839564

Genes

MAPT
CBS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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